rotator cuff tear
Conditions
Interventions
Gold Standard:Arthroscopic results of the shoulder, including rotator cuff tear type, morphology, and residual tendon quality, were the gold standard.
Index test:Philips ultrasound instrument, 4~15MHz high-frequency linear array probe, 3~14MHz three-dimensional volume probe
Esaote MyLab ultrasonic instrument, 4~13MHz linear array probe
Mindray ultrasonic instrument, 3~11MHz linear array probe
Sponsors
Chinese PLA General Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: The patient had shoulder pain, shoulder joint dysfunction and was suspected to have rotator cuff tear and was hospitalized for shoulder arthroscopic repair.
Exclusion criteria
Exclusion criteria: Patients with shoulder pain without rotator cuff tear; Previous surgical history, non-invasive treatment including NSAID and PRP therapy and/or regular exercise and/or physical therapy (TENS, ultrasound, etc.) for at least 2 months; Allergic reaction to disinfectants, anesthetics, sodium citrate and calcium chloride; Thrombocytopenia, acute and chronic infection, anticoagulant therapy, etc. Previous adverse reactions (hypertension, systemic allergy and hypersensitivity, and even severe kidney or liver diseases) occurred after local injection; Pregnancy and malignant tumors occurred within 6-12 weeks after minimally invasive treatment. Patients with severe osteoporosis near the joints; Patients unable to maintain follow-up or provide informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Two-dimensional ultrasound;Three-dimensional ultrasound;Contrast-enhanced ultrasound;Shear wave elastography;Arthroscopy; | — |
Countries
China
Contacts
Public ContactWang Yuexiang
Chinese PLA General Hospital
Outcome results
None listed